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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does TUCATINIB Cause Hepatic function abnormal? 35 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Hepatic function abnormal have been filed in association with TUCATINIB (TUKYSA). This represents 0.6% of all adverse event reports for TUCATINIB.

35
Reports of Hepatic function abnormal with TUCATINIB
0.6%
of all TUCATINIB reports
7
Deaths
17
Hospitalizations

How Dangerous Is Hepatic function abnormal From TUCATINIB?

Of the 35 reports, 7 (20.0%) resulted in death, 17 (48.6%) required hospitalization, and 1 (2.9%) were considered life-threatening.

Is Hepatic function abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TUCATINIB. However, 35 reports have been filed with the FAERS database.

What Other Side Effects Does TUCATINIB Cause?

Diarrhoea (1,587) Nausea (862) Fatigue (843) Vomiting (483) Death (400) Off label use (392) Malignant neoplasm progression (361) Palmar-plantar erythrodysaesthesia syndrome (355) Product dose omission issue (332) Asthenia (322)

What Other Drugs Cause Hepatic function abnormal?

NIVOLUMAB (1,131) PEMBROLIZUMAB (1,079) METHOTREXATE (1,054) CABOZANTINIB S-MALATE (912) CYCLOPHOSPHAMIDE (824) BEVACIZUMAB (769) PACLITAXEL (603) LENVATINIB (528) ATORVASTATIN (520) CYCLOSPORINE (508)

Which TUCATINIB Alternatives Have Lower Hepatic function abnormal Risk?

TUCATINIB vs TUCIDINOSTAT TUCATINIB vs TYKERB TUCATINIB vs TYLENOL TUCATINIB vs TYROTHRICIN TUCATINIB vs TYSABRI

Related Pages

TUCATINIB Full Profile All Hepatic function abnormal Reports All Drugs Causing Hepatic function abnormal TUCATINIB Demographics